Simple and efficient access to the left-hand segment of azinomycins
- 1 January 1992
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Journal of the Chemical Society, Perkin Transactions 1
- No. 16,p. 2053-2054
- https://doi.org/10.1039/p19920002053
Abstract
A practical synthesis of the epoxy carboxylic acid 4, the left-hand segment of azinomycins, and its conversion into the naturally occurring amide 3 have been achieved enantioselectively.Keywords
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